Dongkwang Ceftriaxone 1 gram (Ceftriaxone Sodium Hydrate)
Ceftriaxone Sodium Hydrate 1g
Injections · Prescription medication
Dongkwang Pharmaceutical Co., Ltd.
MFDS item code 199600212 · Notified 1996.04.01 · Insurance code 645900661
Treatment of infections of the respiratory system (pneumonia, bronchitis) and the reproductive system (gonorrhea)
This medication is effective in treating respiratory infections such as pneumonia and bronchitis. It is also used for ear, nose, and throat infections, as well as kidney and urinary tract infections, and reproductive system infections like gonorrhea. It aids in the prevention of sepsis and infections before and after surgery. It can be applied to treat infections of bones and joints, as well as skin and soft tissue infections. It is effective for gastrointestinal infections such as peritonitis, cholecystitis, cholangitis, and infections in immunocompromised patients. Additionally, it is used for the treatment of meningitis, contributing to the improvement of various infections.
In adults and children over 12 years, administer 1–2 g (potency) of ceftriaxone by intravenous or intramuscular injection once daily. For infections caused by severe pathogens or pathogens with moderate susceptibility, the dosage can be increased up to 4 g (potency) once daily. For treatment of gonorrhea, a single intramuscular injection of 250 mg (potency) is recommended. To prevent infections before and after surgery, administer 1–2 g (potency) as a single dose 30 to 90 minutes before the surgery.
In newborns (up to 14 days of age), administer 20–50 mg (potency) per Kg of body weight once daily, not exceeding 50 mg (potency) per Kg. There is no distinction between premature and term infants. Infants and young children.
This medication should not be mixed or administered concurrently with calcium-containing solutions or drugs. Particularly in newborns, there is a risk of precipitation when this drug and calcium combine, so it should not be administered. Patients with hypersensitivity to this drug, or those allergic to cephalosporins or penicillin antibiotics, should not use it. Caution is also required when using it together with drugs containing lidocaine. It should not be administered to premature infants or newborns with bilirubin binding issues. Patients with a history of drug allergies or allergic conditions should use this medication with caution. Patients with reduced kidney function may experience prolonged retention of the drug leading to side effects, necessitating dosage adjustments. Elderly patients or those in poor health also require caution, and regular monitoring and supplementation of vitamin K may be necessary due to potential deficiency. When using this medication, various side effects such as headache, dizziness, rash, diarrhea, liver function abnormalities may occur, and any unusual symptoms should be reported to a physician immediately. In particular, if severe allergic reactions or shock symptoms occur, administration should be stopped immediately, and emergency treatment should be sought. This medication should be used only for the duration necessary to prevent the development of resistant organisms, and it is advisable to perform a skin reaction test before administration. During administration, regular checks of liver, kidney, and blood tests should be conducted to monitor for abnormalities. If given with calcium-containing solutions, precipitation may occur; hence it should not use the same infusion site as calcium solutions. If they must be used together, the infusion site should be thoroughly cleaned before sequential administration. This medication should be used cautiously in pregnant or breastfeeding women as the effects on the fetus or newborn have not been fully established. Newborns or premature infants should not be administered this drug due to the risk of bilirubin encephalopathy. Elderly patients may be more susceptible to side effects due to decreased bodily functions. This medication can affect results of certain clinical tests such as blood glucose tests or urine tests, so the healthcare provider should be informed about the use of this medication during testing. Local reactions like injection site pain or phlebitis may occur, so care should be taken with the method and speed of injection, and it is advisable to administer slowly whenever possible. In case of overdose, there is no specific antidote, so symptomatic treatment should be given. Caution should be taken to watch for symptoms like dizziness during driving or operating machinery while on this medication. Finally, this medication should be used according to the physician's instructions on the proper dosage and administration, and immediate consultation with healthcare providers is necessary if any adverse reactions are suspected.
Hives, severe swelling (edema), difficulty breathing, severe rash with high fever, blisters, skin shedding, pain in oral/ocular mucosa, yellowing of skin or eyes (jaundice), extreme lethargy, sudden severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, markedly reduced urination, severe swelling of the entire body with elevated blood pressure, shock, taste disturbances, wheezing, bowel movement changes, tinnitus.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored tightly sealed in a container after use and kept at a temperature at room temperature between 1 to 30 degrees Celsius. This storage method helps maintain the drug's efficacy and prevent deterioration.
Domestic: A clear, colorless vial injection containing a white to light yellow powder. Export: A colorless vial filled with white to light yellow crystalline powder.
10 vials
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.